510(k) K921183

DIASTAT ANTI-MITOCHONDRIAL ANTIBODY KIT by Shield Diagnostics, Ltd. — Product Code DBM

K921183 is an FDA 510(k) premarket notification submitted by Shield Diagnostics, Ltd. for the device "DIASTAT ANTI-MITOCHONDRIAL ANTIBODY KIT". The FDA issued a decision of Substantially Equivalent on June 19, 1992. The device falls under product code DBM (Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control), a Class II device regulated under 21 CFR 866.5090. Shield Diagnostics, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 19, 1992
Date Received
March 9, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control
Device Class
Class II
Regulation Number
866.5090
Review Panel
IM
Submission Type